NDC 50228-466 – Nabumetone

Nabumetone 750 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC50228-466

Product details

Brand name
Nabumetone
Generic name
Nabumetone
Labeler
ScieGen Pharmaceuticals Inc
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078420
Marketed since
June 26, 2019
Listing expires
December 31, 2026
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Nabumetone →

Package NDC codes (3)

Package NDCDescriptionSince
50228-466-01100 TABLET in 1 BOTTLE (50228-466-01)Jun 26, 2019
50228-466-05500 TABLET in 1 BOTTLE (50228-466-05)Jun 26, 2019
50228-466-3030 TABLET in 1 BOTTLE (50228-466-30)Jun 26, 2019

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